Analysis of the mitochondrial genome in sudden infant death syndrome
Author:
Publisher
Wiley
Subject
General Medicine,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.2003.tb00562.x/fullpdf
Reference12 articles.
1. Mitochondrial DNA point mutations detected in four cases of sudden infant death syndrome;Opdal;Acta Paediatr,1999
2. Increased number of substitutions in the D-loop of mitochondrial DNA in the sudden infant death syndrome;Opdal;Acta Paediatr,1998
3. DNA extraction from formalin-fixed, paraffin-embedded tissues: protein digestion as a limiting step for retrieval of high-quality DNA;Diaz-Cano;Diagn Mol Pathol,1997
4. Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome;Rieder;Nucleic Acids Res,1998
5. MITOMAP: an update on the status of the human mitochondrial genome database;Kogelnik;Nucleic Acids Res,1997
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3. A high number of ‘natural’ mitochondrial DNA polymorphisms in a symptomatic Brugada syndrome type 1 patient;Journal of Genetics;2020-08-04
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